Author/Authors :
-، - نويسنده Biotechnology Research Center, Tabriz University of Medical Sciences, Tabriz, I.R. IRAN
Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, I.R. IRAN Jalalypour, Farzaneh , -، - نويسنده mmunology Research Center, Tabriz University of Medical Sciences, Tabriz, I.R. IRAN Farajnia, Safar , -، - نويسنده Department of Cellular and Molecular Biology, Azarbayjan Shahid Madani University, Tabriz, I.R. IRAN Mahmoudi, Fatemeh , -، - نويسنده Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, I.R. IRAN Baradaran, Behzad , -، - نويسنده Department of Cellular and Molecular Biology, Azarbayjan Shahid Madani University, Tabriz, I.R. IRAN Farajzadeh, Davoud , -، - نويسنده Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, I.R. IRAN Rahbarnia, Leila , -، - نويسنده Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, I.R. IRAN Majidi, Jafar
Abstract :
Background:Epidermal growth factor receptor (EGFR) overexpression is a characteristic of several malignancies and could be considered as an excellent target for designing specific inhibitors such as anti-EGFR monoclonal antibodies for cancer therapy. Drawbacks exerted by large sizes of full-length antibodies have lead to the development of single chain antibodies, which benefit from having smaller sizes and short circulation half-lives. Objectives:The aim of this study was cloning, expression and purification of variable regions of anti-EGFR monoclonal antibody in E. coli for production of single chain antibodies. Materials and Methods:The RNA, extracted from the C225 hybridoma cells, was reverse transcribed into cDNA and used for PCR amplification of genes encoding light and heavy chains from the variable regions. The PCR products were cloned and expressed in E. coli BL21 for production of a single chain antibody. The expressed protein was analyzed by SDS-PAGE and purified by Ni-NTA affinity chromatography. The reactivity of purified C225-scFv with EGFR-expressing A431 tumor cell line was tested by western blotting and enzyme-linked immunosorbent assays. Results:The results indicated that C225-scFv was highly expressed in E. coli and appeared as a protein with a mass of 27 kDa in the sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) analysis of the induced cell lysate. Reactivity analysis of the purified C225-scFv with A431 tumor cell line by western blotting and enzyme linked immune sorbant assay (ELISA) revealed high binding affinity of the recombinant C225-scFv to the target cells. Conclusions:The results of this study indicated that C225-scFv is capable of binding to EGFR and could be considered as a useful tool for diagnosis and treatment of EGFR-overexpressing tumor cells.
